• 약학회지
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• 제31권5호
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• pp.315-321
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• 1987

A high performance liquid chromatographic method was developed for the determination of glycyrrhetinic acid contained in licorice powder. Glycyrrhetinic acid which is hydrolysate of glycyrrhizin extracted from licorice powder, was determined with good result by HPLC using 2-bromoacetyltriphenylene labeling reagent. The glycyrrhetinic acids were labeled with 2-bromoacetyltriphenylene in acetonitrile using 18-crown-6-ether and KOH as a catalyst. Derivatized glycyrrhetinic acids were separated from the extracted licorice powder on a reversed-phase column (chemopak $C_{18}$) using 100% acetonitrile as a mobile phase and monitored by an UV-detector at 268nm. Linearity of calibration curve was obtained between 5 ng and 20 ng, and the lower limit of detection was 2 ng. The recovery of glycyrrhetinic acid to licorice powder was about 99.3%. This method was sensitive, reliable and useful for, determination of glycyrrhetinic acid.

• 한국식품위생안전성학회지
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• 제2권3호
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• pp.89-95
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• 1987

시판 갈근으로부터 Isoflavanoid 성분인 Daidzein과 Daidzin을 분리 정제하고 이를 표준물질로 하여 시판 칡차 8종에 대한 칡성분 분석을 HPLC 방법으로 시도하여 다음과 같은 결론은 얻었다. 1. 칡차의 성분 분석법은 종래의 TLC법에 비하여 HPLC를 이용, 신속하고 정확하게 분석할 수 있었다. 2. 추출방법에 따라 성분함량이 크게 영향을 받아 Daidzein을 분석할 경우는 냉침법이, Daidzin의 분석시는 가열 추출법이 양호하였다. 3. 한국산 갈근중 Daidzein과 Daidzin은 0.08% 및 0.66% 함유되었다. 4. 시판 칡차중 고형차류는 칡의 성분이 표기량에 비하여 매우 적게 함유되거나 전혀 함유되지 않은 예도 있으며 액상차의 경우는 엑기스 고형분이 4∼5%가 함유되었다.

• Journal of Applied Biological Chemistry
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• 제64권1호
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• pp.13-17
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• 2021

Qantitative analysis of six compounds: (+)-catechin, benzoic acid, gallic acid methyl ester, paeonol, paeoniflorin, and albiflorin from Paeonia lactiflora extracts was performed using high-performance liquid chromatography and an ultraviolet (UV) detector, following different extraction methods. A reverse-phase column was used in a gradient elution system, and UV detection was performed at 280 nm. The results showed that the quantity of paeoniflorin was the highest in ethanol and water extracts (73.89 and 57.87 mg/g, respectively) among the six compounds. This study contributes a good analysis method for the contents of P. lactiflora and would be propitious for developing medicines and functional foods.

• 대한화학회지
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• 제37권4호
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• pp.453-461
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• 1993

테프론 코일과 저압 수은 램프를 사용, 간단하게 제작된 광화학 반응기를 이용한 HPLC 검출 방법을 연구하였다. 4종의 티오카바메이트 시료들을검출함에 있어 UV, 형광 및 전기화학 검출기 등에서 광화학 반응을 통한 액체 크로마토그래피 후컬럼 검출법의 유용성을 알아보았다. 액체 크로마토그래피를 통해 분리된 티오카바메이트류에 254nm의 UV을 조사할 경우 4종의 시료는 모두 광반응이 일어나 형광을 통해 분리된 티오카바메이트류에 254nm의 UV을 조사할 경우 4종의 시료는 모두 광반응이 일어나 형광을 나타내거나, 전기화학 검출기에 큰 검출 응답을 나타내었다. UV 검출법의 경우 광반응 생성물은 광반응전보다 검출감도는 감소하였으나 장파장쪽에서 검출이 용이하였다. 형광 검출법의 경우 광반응전 4종의 티오카바메이트는 전혀 검출되지 않았으나, 광반응 후 MPTC,CPTC는 Ph 4.0, 50% 아세토니트릴 이동상 조건에서 5.0~9.3ng의 검출한계를 나타내었다. 전기화학 검출법에서는 광반응전 시료가 매우 작은 검출 응답을 보였고, 광반응 후 시료는 5~20배 이상의 검출감도가 증대되었으며 13.3~0.02ng의 검출한계를 나타내었다. 이때 최적 검출조건은 50% 아세토니트릴 $-0.5{\times}10^{-2}$ M 인산 완충용액, pH 7.0 이었다. 또한 티오카바메이트의 광반응물과 OPA-MERC를 반응 코일내에 유도체를 형성시켜 형광검출기로 검출해냄으로써 광분해물에서 1차 아민이 생성됨을 알 수 있었다.

• 생약학회지
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• 제45권4호
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• pp.294-299
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• 2014

The simultaneous determination of platyphylloside, aceroside and betulin was established for the quality control of Betula platyphylla bark using a high performance liquid chromatography and diode-array UV/Vis detector (HPLC-DAD). Separation and quantification were successfully achieved with a INNO C18 column ($5{\mu}m$, 4.6 mm $I.D.{\times}150mm$) by gradient elution of a mixture of methanol and water at a flow rate of 1.0 ml/min. Validation of the developed method was performed by various factor such as linearity, specificity, precision, accuracy, system suitability and stability. This method was successfully applied to the determination of contents of platyphylloside, aceroside VIII and betulin in three batches of Betula platyphylla bark extract. These results suggest that the developed HPLC method is simple, effective and could be utilized as a quality control method for Betula platyphylla bark products.

• Journal of Pharmaceutical Investigation
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• 제22권4호
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• pp.317-321
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• 1992

A high-performance liquid chromatographic (HPLC) method was developed for the determination of diltiazem (DTZ) and its major metabolite, deacetyldiltiazem (DAD), in rat plasma. DTZ, DAD and imipramine, the internal standard, were selectively fractionated from plasma on a $C_{18}$ reversedphase column $({\mu}-Bondapak,\;10\;{\mu}m\;silica,\;300{\times}3.9\;mm\;ID)$. The composition of the mobile phase was methanol: acetonitrile: 0.04 M ammonium bromide: triethylamine (40:24:36:0.06 in volume). The pH of the mobile phase of their method was lowered to 6.4. The eluents from the column were detected for DTZ and DAD using a UV detector at 237 nm. The recovery was >85% for DTZ and DAD, and average intra-day and inter-day coefficients of variation were <6% for DTZ and DAD at the concentration ranges of 20-1000 ng/ml. Detection limit of DTZ and DAD in plasma was 20 ng/ml with signal-to-noise ratio of 3. This method would be applicable to practical pharmacokinetic studies without detriment to the HPLC column.

• 한국식품위생안전성학회지
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• 제3권4호
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• pp.203-209
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• 1988

식품중 보존료의 분석방법을 신속 간단하면서도 정화기 정량할 수 있는 방법 개발을 시도한 바 다음과 같은 결론을 얻었다. 1. HPLC system에 의한 희석법으로는 간장중 paraben류와 , 유산균음료중 SOA를 99%이상의 회수율로 20분 이내에 정량할 수 있었다. 2. GLC system에 의한 직접 추출법으로 간장중 BA와 Paraben류의 동시정량이 가능하였으며 유산균음료와 SOA를 99%이상의 회수율로 신속히 정량 할 수 있다.

• 생약학회지
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• 제41권4호
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• pp.323-327
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• 2010

A high performance liquid chromatographic (HPLC) method for the simultaneous determination of dictamine, obacunone and fraxinellone was established for the quality control of traditional herb Dictamnus dasycarpus cortex. Separation and quantification were successfully achieved with a Shiseido C18 column ($5\;{\mu}m$, 4.6 mm I.D. ${\times}$ 250 mm) by gradient elution of a mixture of methanol and water at a flow rate of 1.0 ml/min. The diode-array UV/Vis detector (DAD) was used for the detection and the wavelength for quantification was set at 236 nm. The presence of dictamine, obacunone and fraxinellone in this extract was ascertained by retention time, spiking with each authentic standard and UV spectrum. All three compounds showed good linearity ($r^2$ > 0.999) in relatively wide concentration ranges. The R.S.D. recovery of each compound was 101.0~103.7% with R.S.D. values less than 1.0%. This method was successfully applied to the determination of contents of dictamine, obacunone and fraxitnellone in three commercial products of D. dasycarpus cortex. These results suggest that the developed HPLC method is simple, effective and could be readily utilized as a quality control method for commercial products.

• 한국축산식품학회지
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• 제32권5호
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• pp.571-577
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• 2012

This study was carried out to develop an analytical method for the determination of vitamin D in infant formula. Vitamin D was determined by column-switching high-performance liquid chromatography (HPLC) equipped with a reversed phase column and UV detector after saponification and extraction of the formula with an organic solvent. A preseparation column ($C_8$), focusing column ($C_{18}$), analytical column ($C_{18}$) and UV-Vis detector (254 nm) were used. The limits of detection (LOD) and the limits of quantification (LOQ) for vitamin D were estimated to be $1.51{\mu}g/kg$ and $4.95{\mu}g/kg$, respectively. The linearity, recovery, precision and accuracy of the analytical method for vitamin D were evaluated through the application of a SRM (Standard Reference Material) 1846 (National Institute of Standard & Technology, USA). The linearity of this method was calculated with a value of the coefficient of determination ($r^2$) ${\geq}0.9999$. The recovery of vitamin D was $85.20{\pm}3.00%$. The intra-assay precision for vitamin D was between $1.68{\pm}0.03%$ and $5.75{\pm}0.33%$, and the inter-assay precision for vitamin D ranged from $1.73{\pm}0.03%$ to $2.96{\pm}0.09%$. The intra-assay accuracy for vitamin D was between $100.03{\pm}2.77%$ and $102.01{\pm}0.59%$, and the inter-assay accuracy for vitamin D ranged from $99.00{\pm}1.53%$ to $102.01{\pm}3.04%$. The proposed method is optimal for the separation and quantification of vitamin D from infant formula.

• Journal of Preventive Veterinary Medicine
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• 제42권4호
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• pp.171-176
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• 2018

A study of the tissue depletion of florfenicol (FFC) administered orally to pigs at a dose of 0.05 kg/ton feed for 7 days was performed. Sixteen healthy cross swine were administered with FFC. Four treated animals were arbitrarily selected to be sacrificed 1, 3 and 5 days after the end of treatment. FFC residue concentrations in muscle, liver, kidney, and fat were determined using high-performance liquid chromatography (HPLC) with ultraviolet photometric detector at 230 nm. The correlation coefficient ($R^2$) of the calibration curve for florfenicol amine (FFCa) was > 0.997 and the limits of detection and quantification were 0.012 and $0.040{\mu}g/mL$, respectively. Recovery rates in swine edible tissues ranged from 79.1 to 93.5%. In the FFC-treated group, FFC residues at 3 days post-treatment were below the maximum residue limits (MRLs) in muscle, kidney and fat, and those at 5 days post-administration were below the MRLs in all edible tissues. These results suggest that the withdrawal period of FFC after the drug treatment might be 5 days, which is a sufficient amount of time for reduction of the FFC residues below the MRLs in all edible tissues.